Canonical Allele Identifier: CA433532850

Gene: COL7A1

Linked Data

• MyVariant Identifiers: chr3:g.48605179T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48567746T>A , CM000665.2:g.48567746T>A	GRCh38
NC_000003.11:g.48605179T>A , CM000665.1:g.48605179T>A	GRCh37
NC_000003.10:g.48580183T>A	NCBI36
NG_007065.1:g.32507A>T , LRG_286:g.32507A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000681320.1:c.7947A>T MANE Select	ENSP00000506558.1:p.Pro2649=
ENST00000328333.12:c.7947A>T	ENSP00000332371.8:p.Pro2649=
ENST00000459756.5:n.770A>T
ENST00000487017.5:n.4586A>T
NM_000094.3:c.7947A>T , LRG_286t1:c.7947A>T	NP_000085.1:p.Pro2649=
XM_011533336.1:c.7974A>T	XP_011531638.1:p.Pro2658=
XM_011533337.1:c.7947A>T	XP_011531639.1:p.Pro2649=
XM_011533338.1:c.7914A>T	XP_011531640.1:p.Pro2638=
XR_940369.1:n.8010A>T
XR_940370.1:n.8010A>T
XR_940371.1:n.8010A>T
XM_017005688.1:c.7887A>T	XP_016861177.1:p.Pro2629=
XR_001740003.1:n.7983A>T
XR_001740004.1:n.7983A>T
XR_001740005.1:n.7983A>T
NM_000094.4:c.7947A>T MANE Select	NP_000085.1:p.Pro2649=